Stem cells are natural units of tissue repair and homeostasis. Recent studies suggest that stem cells may be more versatile than previously appreciated. This property holds promise for tissue regeneration, particularly for less controversial adult stem cells. Our global objective is to develop strategies for the isolation, purification and characterization of multipotent adult skin stem cells and their transitamplifying progeny. While skin keratinocytes are one of the few adult stem cells that can be maintained and propagated in vitro, their identification and isolation have been hampered by the lack of reliable markers that distinguish stem cells from their progeny. Without this information, the stress of removing stem cells from their niche make it impossible to assess at what point these cells might cease to function as multipotent stem cells. Here, we propose a novel strategy for purification of multipotent adult murine skin stem cells from their natural niche, by taking advantage of the slow-cycling properties and the few known markers preferentially expressed in these cells. We also devise strategies for purifying three different transit-amplifying progeny of these cells. We will determine and compare the global expression patterns of these cell populations and employ these and known markers to examine how skin stem cells change programs of gene expression during both embryonic development, and postnatally, in natural homeostasis, with the hair cycle, in response to injury or tumorigenesis, and when placed in culture. Finally, we will use this information to explore the functional consequences of altering the expression programs of key genes, which distinguish skin stem cells from their non-stem lineages. Taken together, these studies are expected to provide new and important insights into understanding how skin stem cells possess and maintain their unique self-renewing properties, and how they adopt different fates, including epidermal and hair follicle differentiation. This research is a fundamental prerequisite to ascertaining the potential of skin stem cells for therapeutic purposes that go beyond their present use in providing long-term engraftment on burn patients.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Project (R01)
Project #
1R01AR050452-01
Application #
6705196
Study Section
Special Emphasis Panel (ZRG1-GMA-1 (01))
Program Officer
Moshell, Alan N
Project Start
2004-02-26
Project End
2008-11-30
Budget Start
2004-02-26
Budget End
2004-11-30
Support Year
1
Fiscal Year
2004
Total Cost
$355,625
Indirect Cost
Name
Rockefeller University
Department
Biology
Type
Other Domestic Higher Education
DUNS #
071037113
City
New York
State
NY
Country
United States
Zip Code
10065
Keyes, Brice E; Fuchs, Elaine (2018) Stem cells: Aging and transcriptional fingerprints. J Cell Biol 217:79-92
Sonobe, Yoshifumi; Ghadge, Ghanashyam; Masaki, Katsuhisa et al. (2018) Translation of dipeptide repeat proteins from the C9ORF72 expanded repeat is associated with cellular stress. Neurobiol Dis 116:155-165
Naik, Shruti; Larsen, Samantha B; Cowley, Christopher J et al. (2018) Two to Tango: Dialog between Immunity and Stem Cells in Health and Disease. Cell 175:908-920
Ge, Yejing; Fuchs, Elaine (2018) Stretching the limits: from homeostasis to stem cell plasticity in wound healing and cancer. Nat Rev Genet 19:311-325
Naik, Shruti; Larsen, Samantha B; Gomez, Nicholas C et al. (2017) Inflammatory memory sensitizes skin epithelial stem cells to tissue damage. Nature 550:475-480
Ge, Yejing; Gomez, Nicholas C; Adam, Rene C et al. (2017) Stem Cell Lineage Infidelity Drives Wound Repair and Cancer. Cell 169:636-650.e14
Gonzales, Kevin Andrew Uy; Fuchs, Elaine (2017) Skin and Its Regenerative Powers: An Alliance between Stem Cells and Their Niche. Dev Cell 43:387-401
Sartaj, R; Zhang, C; Wan, P et al. (2017) Characterization of slow cycling corneal limbal epithelial cells identifies putative stem cell markers. Sci Rep 7:3793
Lu, Catherine P; Polak, Lisa; Keyes, Brice E et al. (2016) Spatiotemporal antagonism in mesenchymal-epithelial signaling in sweat versus hair fate decision. Science 354:
Keyes, Brice E; Liu, Siqi; Asare, Amma et al. (2016) Impaired Epidermal to Dendritic T Cell Signaling Slows Wound Repair in Aged Skin. Cell 167:1323-1338.e14

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